HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Naphthol → 1-(alpha-Naphthoxy)-2-benzyloxy-3-(iso-propylamino)-propane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Naphthol | HCID 7005 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-(Iso-propyl)-3-benzyloxyazetidine | HCID 20517324 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(alpha-Naphthoxy)-2-benzyloxy-3-(iso-propylamino)-propane | HCID 13055708 | 79% |
Reaction Conditions
| Temperature | 200 °C |
|---|
Reaction Steps
To a mixture of 6.2 parts of 1-(iso-propyl)-3-benzyloxyazetidine and 43 parts of α-naphthol 1.5 parts of sodium hydroxide was added, and the mixture was heated at 200° C. for 16 hours. The reaction mixture was cooled, and 100 parts of ether were added thereto. Excessive α-naphthol was removed by extraction with 2 N-sodium hydroxide aqueous solution. The remaining ether layer was washed in water and dried over anhydrous sodium sulfate. After distillation of ether, the residue was subjected to distillation to yield 8.3 parts of 1-(α-naphthoxy)-2-benzyloxy-3-(iso-propylamino)-propane boiling at 192°-195° C. The yield was 79%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04360464 |
| Source dataset | uspto-grants-1982_11 |
| ORD ID | ord-a58a529d3dcc43d5b190b38142ae8bec |
| Source note | uspto-grants-1982_11 |